# FDA Inspection 655743 - Kanec Usa, Inc. - April 19, 2010

Source: https://www.keypedia.com/records/fda_inspections/kanec-usa-inc/272cefef-4fa8-437d-8fbe-bbf63676be12
Source feed: FDA_Inspections

> FDA Inspection 655743 for Kanec Usa, Inc. on April 19, 2010. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 655743
- Company Name: Kanec Usa, Inc.
- Inspection Date: 2010-04-19
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 655743 - 2010-04-19](https://www.keypedia.com/records/fda_inspections/kanec-usa-inc/a310052c-564c-43ed-83b2-1af5b91bd049)
- [FDA Inspection 655743 - 2010-04-19](https://www.keypedia.com/records/fda_inspections/kanec-usa-inc/095c61b1-ac98-4db4-9b01-07abd98d9084)
- [FDA Inspection 655743 - 2010-04-19](https://www.keypedia.com/records/fda_inspections/kanec-usa-inc/c121ceda-2cfd-4da1-9a1d-ef9b5a86696d)

Company: https://www.keypedia.com/companies/kanec-usa-inc/96a91f74-bad9-4bef-b118-65249ed95aab

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7